ID
42672
Beschreibung
This form contains the eligibility criteria. To be assessed at screening. Study ID: 103629 Clinical Study ID: TRX103629 Study Title: An open-label, randomized, 3-period crossover study to evaluate sumatriptan and naproxen pharmacokinetics for a combination tablet product containing sumatriptan/naproxen sodium followed by IMITREX™ (sumatriptan succinate) Injection 4mg administered using the IMITREX STATdose System and a sumatriptan/naproxen sodium tablet followed by IMITREX (sumatriptan succinate) Injection 6mg administered using the STATdose system compared with an IMITREX tablet 100mg followed by an IMITREX tablet 100mg Patient Level Data: Study Listed on ClinicalStudyDataRequest.com Clinicaltrials.gov Identifier: NCT00875784 Clinicaltrials.gov link: https://clinicaltrials.gov/ct2/show/NCT00875784 Sponsor: GlaxoSmithKline Collaborators: N/A Phase: phase 1 Study Recruitment Status: Completed Generic Name: sumatriptan Trade Name: Imitrex ,Imiject ,Imigran; Imitrex,Imiject,Imigran Study Indication: Migraine Disorders Other Eligibility Criteria Considerations To assess any potential impact on subject eligibility with regard to safety, the investigator must refer to the following document(s) for detailed information regarding warnings, precautions, contraindications, adverse events, and other significant data pertaining to the investigational product(s) being used in this study: approved product label for IMITREX injection and tablets, approved product label for naproxen sodium tablets and CIB for the combination product (sumatriptan/naproxen sodium).
Link
https://clinicaltrials.gov/ct2/show/NCT00875784
Stichworte
Versionen (3)
- 17.11.18 17.11.18 -
- 21.11.18 21.11.18 -
- 17.09.21 17.09.21 -
Rechteinhaber
GlaxoSmithKline
Hochgeladen am
17. September 2021
DOI
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Lizenz
Creative Commons BY-NC 3.0
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Sumatriptan pharmacokinetics for TREXIMA/IMITREX NCT00875784
Eligibility Criteria
- StudyEvent: ODM
Beschreibung
Eligibility Question
Alias
- UMLS CUI-1
- C1516637
Beschreibung
Inclusion Criteria
Alias
- UMLS CUI-1
- C1512693
- UMLS CUI-2
- C1516637
Beschreibung
Healthy subjects are defined as individuals who are free from clinically significant illness or disease as determined by their medical history, physical examination, laboratory studies and other tests.
Datentyp
boolean
Alias
- UMLS CUI [1]
- C3898900
- UMLS CUI [2]
- C1519386
- UMLS CUI [3]
- C0001779
- UMLS CUI [4]
- C0079399
Beschreibung
Females of non-childbearing potential or of childbearing potential with negative pregnancy test and using certain contraceptive method(s)
Datentyp
boolean
Alias
- UMLS CUI [1]
- C3831118
- UMLS CUI [2]
- C0700589
- UMLS CUI [3]
- C0427780
Beschreibung
Stable regimen of oral contraceptives
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0009905
- UMLS CUI [1,2]
- C0237125
- UMLS CUI [1,3]
- C0205360
Beschreibung
BMI: 20-32 kg/m2
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1305855
Beschreibung
QTc <450 msec or <480 msec if associated with bundle branch block
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0489625
- UMLS CUI [1,2]
- C0006384
Beschreibung
Willing and able to provide written informed consent
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0021430
- UMLS CUI [1,2]
- C0600109
Beschreibung
Exclusion Criteria
Alias
- UMLS CUI-1
- C0680251
Beschreibung
Migraine attacks
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0149931
Beschreibung
Confirmed or suspected ischemic heart disease (angina pectoris, history of myocardial infarction, documented silent ischemia), Prinzmetal's angina/coronary vasospasm
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0002962
- UMLS CUI [1,2]
- C0750491
- UMLS CUI [2,1]
- C0002962
- UMLS CUI [2,2]
- C0750484
- UMLS CUI [3,1]
- C0027051
- UMLS CUI [3,2]
- C0750491
- UMLS CUI [4,1]
- C0027051
- UMLS CUI [4,2]
- C0750484
- UMLS CUI [5,1]
- C0340291
- UMLS CUI [5,2]
- C0750491
- UMLS CUI [6,1]
- C0340291
- UMLS CUI [6,2]
- C0750484
- UMLS CUI [7,1]
- C0002963
- UMLS CUI [7,2]
- C0750491
- UMLS CUI [8,1]
- C0002963
- UMLS CUI [8,2]
- C0750484
Beschreibung
Ischemic abdominal syndromes, peripheral vascular disease or Raynaud’s Syndrome
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0034734
- UMLS CUI [2]
- C0085096
- UMLS CUI [3,1]
- C0022116
- UMLS CUI [3,2]
- C0000726
Beschreibung
Cardiac arrhythmias requiring medication or a history of clinically significant electrocardiogram abnormality contraindicating the study participation
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0003811
- UMLS CUI [1,2]
- C1514873
- UMLS CUI [1,3]
- C0013227
- UMLS CUI [2,1]
- C0522055
- UMLS CUI [2,2]
- C2985739
- UMLS CUI [2,3]
- C1301624
- UMLS CUI [2,4]
- C2348568
Beschreibung
History of cerebrovascular pathology including stroke and/or transient ischemic attacks
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0007820
- UMLS CUI [2]
- C0559159
- UMLS CUI [3]
- C0007787
Beschreibung
Congenital heart disease
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0152021
Beschreibung
Hypertension at screening
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1868885
- UMLS CUI [2]
- C0871470
- UMLS CUI [3]
- C0428883
Beschreibung
Likely to have unrecognized cardiovascular or cerebrovascular disease (e.g. risk factors such as hypertension, hypercholesterolemia, prior smoking history, obesity, diabetes, strong family history of coronary artery disease, female with surgical or physiological menopause, or male over 40 years of age
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0007222
- UMLS CUI [1,2]
- C4288068
- UMLS CUI [2,1]
- C0007820
- UMLS CUI [2,2]
- C4288068
- UMLS CUI [3]
- C0020538
- UMLS CUI [4]
- C0020443
- UMLS CUI [5]
- C1519384
- UMLS CUI [6]
- C0028754
- UMLS CUI [7]
- C0011849
- UMLS CUI [8,1]
- C0241889
- UMLS CUI [8,2]
- C1956346
- UMLS CUI [9,1]
- C0086287
- UMLS CUI [9,2]
- C0025320
- UMLS CUI [10,1]
- C0001779
- UMLS CUI [10,2]
- C0086582
Beschreibung
History of epilepsy or structural brain lesions lowering the convulsive threshold or recent treatment with an antiepileptic drug
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0455511
- UMLS CUI [2,1]
- C0221505
- UMLS CUI [2,2]
- C0234976
- UMLS CUI [3,1]
- C0003299
- UMLS CUI [3,2]
- C0332185
Beschreibung
History of impaired hepatic or renal function
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0086565
- UMLS CUI [2]
- C1565489
Beschreibung
Herbal preparations containing St. John's Wort (Hypericum perforatum) currently or recently taken
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0521116
- UMLS CUI [1,2]
- C1360419
- UMLS CUI [1,3]
- C0332256
- UMLS CUI [1,4]
- C0936242
- UMLS CUI [2,1]
- C0332185
- UMLS CUI [2,2]
- C1360419
- UMLS CUI [2,3]
- C0332256
- UMLS CUI [2,4]
- C0936242
Beschreibung
Use of other prescription or non-prescription drugs, vitamins, herbal and dietary supplements, excluded acetaminophen at certain doses and contraceptives
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0013231
- UMLS CUI [2]
- C0304227
- UMLS CUI [3]
- C0042890
- UMLS CUI [4]
- C1504473
- UMLS CUI [5]
- C0242295
- UMLS CUI [6,1]
- C0332300
- UMLS CUI [6,2]
- C0000970
- UMLS CUI [7,1]
- C0332300
- UMLS CUI [7,2]
- C0009871
Beschreibung
History of hypersensitivity, intolerance or contraindication to the use of sumatriptan or naproxen sodium or any of their components or aspirin or any other 5-HT1 receptor agonist.
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0075632
- UMLS CUI [2,1]
- C0277585
- UMLS CUI [2,2]
- C0075632
- UMLS CUI [3,1]
- C1301624
- UMLS CUI [3,2]
- C0075632
- UMLS CUI [4,1]
- C0020517
- UMLS CUI [4,2]
- C0027396
- UMLS CUI [5,1]
- C0277585
- UMLS CUI [5,2]
- C0027396
- UMLS CUI [6,1]
- C0020517
- UMLS CUI [6,2]
- C0027396
- UMLS CUI [7,1]
- C1301624
- UMLS CUI [7,2]
- C0027396
- UMLS CUI [8,1]
- C0020517
- UMLS CUI [8,2]
- C0004057
- UMLS CUI [9,1]
- C0277585
- UMLS CUI [9,2]
- C0004057
- UMLS CUI [10,1]
- C1301624
- UMLS CUI [10,2]
- C0004057
- UMLS CUI [11,1]
- C0020517
- UMLS CUI [11,2]
- C0162754
- UMLS CUI [12,1]
- C0277585
- UMLS CUI [12,2]
- C0162754
- UMLS CUI [13,1]
- C1301624
- UMLS CUI [13,2]
- C0162754
Beschreibung
Gastrointestinal surgery due to bleeding, ulceration or perforation
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1963975
- UMLS CUI [1,2]
- C0543467
- UMLS CUI [2,1]
- C0017181
- UMLS CUI [2,2]
- C0543467
- UMLS CUI [3,1]
- C0151664
- UMLS CUI [3,2]
- C0543467
Beschreibung
History of gastric bypass or stapling surgery
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0149701
- UMLS CUI [2]
- C0017125
Beschreibung
History of GI ulceration or gastrointestinal bleeding
Datentyp
boolean
Alias
- UMLS CUI [1]
- C1963975
- UMLS CUI [2]
- C0017181
Beschreibung
History of inflammatory bowel disease
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0021390
Beschreibung
Recent treatment with an investigational drug
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0304229
- UMLS CUI [1,2]
- C0332185
Beschreibung
Positive serum beta-hCG test (females)
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C1255526
- UMLS CUI [1,2]
- C1446409
- UMLS CUI [1,3]
- C0086287
Beschreibung
Pregnant, actively trying to become pregnant or breast-feeding
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0032961
- UMLS CUI [2]
- C0006147
- UMLS CUI [3]
- C0032992
Beschreibung
History of drug or alcohol abuse
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0262926
- UMLS CUI [1,2]
- C0038586
Beschreibung
Regular Alcohol consumption as measured by alcohol units/week
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0001948
- UMLS CUI [1,2]
- C0205272
- UMLS CUI [2]
- C0560579
Beschreibung
Positive urine drug screening including alcohol
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0743300
- UMLS CUI [2]
- C1112219
Beschreibung
Infection status of hepatitis B, hepatitis C and HIV
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0149709
- UMLS CUI [2]
- C0281863
- UMLS CUI [3]
- C0019699
Beschreibung
Donation of blood
Datentyp
boolean
Alias
- UMLS CUI [1]
- C0005794
Beschreibung
Recent use of tobacco
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0543414
- UMLS CUI [1,2]
- C0332185
Beschreibung
History of sensitivity to heparin, heparin-induced thrombocytopenia or sensitivity the study medications or components
Datentyp
boolean
Alias
- UMLS CUI [1,1]
- C0020517
- UMLS CUI [1,2]
- C0019134
- UMLS CUI [2,1]
- C0262926
- UMLS CUI [2,2]
- C0272285
- UMLS CUI [3,1]
- C0020517
- UMLS CUI [3,2]
- C1521826
Ähnliche Modelle
Eligibility Criteria
- StudyEvent: ODM
C1519386 (UMLS CUI [2])
C0001779 (UMLS CUI [3])
C0079399 (UMLS CUI [4])
C0700589 (UMLS CUI [2])
C0427780 (UMLS CUI [3])
C0237125 (UMLS CUI [1,2])
C0205360 (UMLS CUI [1,3])
C0006384 (UMLS CUI [1,2])
C0600109 (UMLS CUI [1,2])
C0750491 (UMLS CUI [1,2])
C0002962 (UMLS CUI [2,1])
C0750484 (UMLS CUI [2,2])
C0027051 (UMLS CUI [3,1])
C0750491 (UMLS CUI [3,2])
C0027051 (UMLS CUI [4,1])
C0750484 (UMLS CUI [4,2])
C0340291 (UMLS CUI [5,1])
C0750491 (UMLS CUI [5,2])
C0340291 (UMLS CUI [6,1])
C0750484 (UMLS CUI [6,2])
C0002963 (UMLS CUI [7,1])
C0750491 (UMLS CUI [7,2])
C0002963 (UMLS CUI [8,1])
C0750484 (UMLS CUI [8,2])
C0085096 (UMLS CUI [2])
C0022116 (UMLS CUI [3,1])
C0000726 (UMLS CUI [3,2])
C1514873 (UMLS CUI [1,2])
C0013227 (UMLS CUI [1,3])
C0522055 (UMLS CUI [2,1])
C2985739 (UMLS CUI [2,2])
C1301624 (UMLS CUI [2,3])
C2348568 (UMLS CUI [2,4])
C0559159 (UMLS CUI [2])
C0007787 (UMLS CUI [3])
C0871470 (UMLS CUI [2])
C0428883 (UMLS CUI [3])
C4288068 (UMLS CUI [1,2])
C0007820 (UMLS CUI [2,1])
C4288068 (UMLS CUI [2,2])
C0020538 (UMLS CUI [3])
C0020443 (UMLS CUI [4])
C1519384 (UMLS CUI [5])
C0028754 (UMLS CUI [6])
C0011849 (UMLS CUI [7])
C0241889 (UMLS CUI [8,1])
C1956346 (UMLS CUI [8,2])
C0086287 (UMLS CUI [9,1])
C0025320 (UMLS CUI [9,2])
C0001779 (UMLS CUI [10,1])
C0086582 (UMLS CUI [10,2])
C0221505 (UMLS CUI [2,1])
C0234976 (UMLS CUI [2,2])
C0003299 (UMLS CUI [3,1])
C0332185 (UMLS CUI [3,2])
C1565489 (UMLS CUI [2])
C1360419 (UMLS CUI [1,2])
C0332256 (UMLS CUI [1,3])
C0936242 (UMLS CUI [1,4])
C0332185 (UMLS CUI [2,1])
C1360419 (UMLS CUI [2,2])
C0332256 (UMLS CUI [2,3])
C0936242 (UMLS CUI [2,4])
C0304227 (UMLS CUI [2])
C0042890 (UMLS CUI [3])
C1504473 (UMLS CUI [4])
C0242295 (UMLS CUI [5])
C0332300 (UMLS CUI [6,1])
C0000970 (UMLS CUI [6,2])
C0332300 (UMLS CUI [7,1])
C0009871 (UMLS CUI [7,2])
C0075632 (UMLS CUI [1,2])
C0277585 (UMLS CUI [2,1])
C0075632 (UMLS CUI [2,2])
C1301624 (UMLS CUI [3,1])
C0075632 (UMLS CUI [3,2])
C0020517 (UMLS CUI [4,1])
C0027396 (UMLS CUI [4,2])
C0277585 (UMLS CUI [5,1])
C0027396 (UMLS CUI [5,2])
C0020517 (UMLS CUI [6,1])
C0027396 (UMLS CUI [6,2])
C1301624 (UMLS CUI [7,1])
C0027396 (UMLS CUI [7,2])
C0020517 (UMLS CUI [8,1])
C0004057 (UMLS CUI [8,2])
C0277585 (UMLS CUI [9,1])
C0004057 (UMLS CUI [9,2])
C1301624 (UMLS CUI [10,1])
C0004057 (UMLS CUI [10,2])
C0020517 (UMLS CUI [11,1])
C0162754 (UMLS CUI [11,2])
C0277585 (UMLS CUI [12,1])
C0162754 (UMLS CUI [12,2])
C1301624 (UMLS CUI [13,1])
C0162754 (UMLS CUI [13,2])
C0543467 (UMLS CUI [1,2])
C0017181 (UMLS CUI [2,1])
C0543467 (UMLS CUI [2,2])
C0151664 (UMLS CUI [3,1])
C0543467 (UMLS CUI [3,2])
C0017125 (UMLS CUI [2])
C0017181 (UMLS CUI [2])
C0332185 (UMLS CUI [1,2])
C1446409 (UMLS CUI [1,2])
C0086287 (UMLS CUI [1,3])
C0006147 (UMLS CUI [2])
C0032992 (UMLS CUI [3])
C0038586 (UMLS CUI [1,2])
C0205272 (UMLS CUI [1,2])
C0560579 (UMLS CUI [2])
C1112219 (UMLS CUI [2])
C0281863 (UMLS CUI [2])
C0019699 (UMLS CUI [3])
C0332185 (UMLS CUI [1,2])
C0019134 (UMLS CUI [1,2])
C0262926 (UMLS CUI [2,1])
C0272285 (UMLS CUI [2,2])
C0020517 (UMLS CUI [3,1])
C1521826 (UMLS CUI [3,2])